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A comparative evaluation of passive and active samplers for measurements of gaseous semi-volatile organic compounds in the tropical atmosphere
Authors:Jun He  Rajasekhar Balasubramanian
Affiliation:1. State Key Laboratory for Biocontrol, School of Life Sciences, Sun Yat-Sen University, Guangzhou 510275, China;2. Center for Environmental Health Research, South China Institute of Environmental Sciences, Ministry of Environmental Protection, Guangzhou 510655, China;3. State Key Laboratory of Organic Geochemistry and Guangdong Key Laboratory of Environmental Resources Utilization and Protection, Guangzhou Institute of Geochemistry, Chinese Academy of Sciences, Guangzhou 510640, China;1. Department of Ecology, College of Urban and Environmental Sciences, Key Laboratory for Earth Surface Processes of the Ministry of Education, Peking University, 5 Yiheyuan Rd., Beijing 100871, China;2. Key Laboratory of Adaptation and Evolution of Plateau Biota, Northwest Institute of Plateau Biology, Chinese Academy of Sciences, 23 Xinning Rd., Xining 810008, China;3. State Key Laboratory of Vegetation and Environmental Change, Institute of Botany, Chinese Academy of Sciences, 20 Nanxincun, Xiangshan, Beijing 100093, China;4. Key Laboratory of Ecosystem Network Observation and Modeling, Synthesis Research Center of Chinese Ecosystem Research Network, Institute of Geographic Sciences and Natural Resources Research, Chinese Academy of Sciences, Beijing 100101, China;5. Center for Global Environmental Research, National Institute for Environmental Studies, Tsukuba, Ibaraki 305-8506, Japan;1. State Key Laboratory of Pollution Control and Resource Reuse, School of the Environment, Nanjing University, Nanjing 210046, PR China;2. Soil and Water Science Department, University of Florida, Gainesville, FL 32611, United States;1. RECETOX Research Centre for Toxic Compounds in the Environment, Faculty of Science, Masaryk University, Kamenice 753/5, Pavilion A29, 625 00 Brno, Czech Republic;2. Department of Physical, Earth and Environmental Sciences, University of Siena, Via Mattioli 4, 53100, Siena, Italy;3. Facultad de Ciencias, Universidad Católica Santísima Concepción, Alonso de Ribera 2850, P.C. 407 01 29 Concepción, Chile
Abstract:The polyurethane foam (PUF) disk-based passive air samplers (PAS), mounted inside two aluminium bowls to buffer the air flow to the disk and to shield it from precipitation and sunlight, were used for the collection of atmospheric SVOCs in Singapore during April 2008–June 2008. Data obtained from PAS measurements are compared to those from active high-volume air sampling (AAS). Single factor ANOVA tests show that there were no significant differences in chemical distribution profiles between actively and passively collected samples (PAHs, F = 3.38 × 10?8 < Fcritical = 4.17 with p > 0.05; OCPs, F = 2.71 × 10?8 < Fcritical = 4.75 with p > 0.05). The average air-side mass transfer coefficient (kA) for PAS, determined from the loss of depuration compounds such as 13C6 – HCB (1000 ng), 13C12 – 4,4′ DDT (1000 ng) and 13C12 – PCB 101 (1000 ng)spiked on the disks prior to deployment, was 0.12 ± 0.04 m s?1. These values are comparable to those reported previously in the literature. The average sampling rate was 3.78 ± 1.83 m3 d?1 for the 365 cm2 PUF disk. Throughout the entire sampling period (~68 d), most of the PAHs and all OCPs exhibited a linear uptake trend on PAS, while naphthalene, acenaphthylene, acenaphthene and fluorene reached the curvilinear phase after the first ~30 d exposure. Theoretically estimated times to equilibrium (teq) ranged from around one month for Acy to hundreds of years for DB(ah)A. Sampling rates, based on the time integrated active sampling-derived concentrations and masses collected by PUF disks during the linear uptake phase, were determined for all target compounds with the average values of 2.50 m3 d?1 and 3.43 m3 d?1 for PAHs and OCPs, respectively. More variations were observed as compared to those from the depuration study. These variation were most likely due to the difference of physicochemical properties of individual species. Lastly, multiple linear regression models were developed to estimate the log-transformed gaseous concentration of an individual compound in air based on the mass collection rate of the gaseous SVOCs measured using the PAS and the molecular weight (MW) of the particular compound for both PAHs and OCPs, respectively.
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